510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K873387Substantially Equivalent

Video Arthroscope, 1.7Mm X 55 Mm

Arthropedics, Inc., Wallington NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873387 is the FDA 510(k) clearance record for VIDEO ARTHROSCOPE, 1.7MM X 55 MM, a class I device, cleared for Arthropedics, Inc. on under FDA product code HXR (Spatula, Orthopedic). FDA records list 29 510(k) clearances for Arthropedics, Inc., from to . As of , FDA records show no recalls naming K873387.

Clearance record

Decision date
Received
(152 days to decision)
Product code
HXR Spatula, Orthopedic
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Arthropedics, Inc. 111 Lester St., Wallington NJ
Third party review
No

Clearances, product code HXR

Trailing 12 months

FDA records hold no clearances under product code HXR in the trailing twelve months.

FDA records show no clearances under product code HXR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HXR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260